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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
1977-10-20
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pubmed:abstractText |
A boy with mental and growth retardation associated with congenital anomalies has a partial duplication of the distal 4q chromosome region as a result of inheritance of a t(4:20) from his mother. Comparison with twelve other patients from the literature indicates that similar clinical features may be associated with this chromosome change suggesting a partial 4q duplication syndrome.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0003-3995
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
31-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:302670-Abnormalities, Multiple,
pubmed-meshheading:302670-Child,
pubmed-meshheading:302670-Child, Preschool,
pubmed-meshheading:302670-Chromosome Aberrations,
pubmed-meshheading:302670-Chromosomes, Human, 19-20,
pubmed-meshheading:302670-Chromosomes, Human, 4-5,
pubmed-meshheading:302670-Humans,
pubmed-meshheading:302670-Infant,
pubmed-meshheading:302670-Intellectual Disability,
pubmed-meshheading:302670-Male,
pubmed-meshheading:302670-Translocation, Genetic,
pubmed-meshheading:302670-Trisomy
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pubmed:year |
1977
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pubmed:articleTitle |
Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
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